Evidence map›Paper›PMID 24627221›Full record

ArticleNucleic acids research2014

Single nucleotide polymorphism-specific regulation of matrix metalloproteinase-9 by multiple miRNAs targeting the coding exon.

Tyler Duellman, Christopher Warren, Jay Yang

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Review
  6. Effects of microRNAs polymorphism in cancer progression.Medical journal of the Islamic Republic of Iran · 2020
    Review
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  18. Exosomal onco-miRs from serum of patients with adenocarcinoma of the esophagus: comparison of miRNA profiles of exosomes and matching tumor.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Tyler DuellmanMolecular and Cellular Pharmacology Graduate Program, University of Wisconsin, SMI 301, 1300 University Ave., Madison, WI 53706, USA.
Christopher WarrenProteovista LLC, Madison, WI 53719, USA.
Jay YangMolecular and Cellular Pharmacology Graduate Program, University of Wisconsin, SMI 301, 1300 University Ave., Madison, WI 53706, USA Department of Anesthesiology, University of Wisconsin, Madison, WI 53706, USA Jyang75@wisc.edu.
University of Wisconsin–Madison · USProteovista (United States) · US

Funding

Training Program in Translational Cardiovascular Science (TPTCS)T32HL007936 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Lee Lochbaum Eckhardt, Gail A Robertson · 2001 to 2026
$11.6M
Training Program In Molecular AND Cellular PharmacologyT32GM008688 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI AUDHYA, ANJON · 1998 to 2020
$6.0M
Ubiquitin-like protein modification in diabetic cardiomyopathyR01HL108551 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ABE, JUN-ICHI, YANG, JAY · 2011 to 2014
$1.6M
Treatment for neuropathic pain targeting selective inhibition of MEKR01GM105665 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI YANG, JAY · 2014 to 2017
$1.1M
Sigma 1 receptor as a master regulator of pronociceptive protein trafficking in tR01GM107054 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI RUOHO, ARNOLD EINO, YANG, JAY · 2013 to 2016
$1.1M
NHLBI NIH HHS R01HL108551NHLBI NIH HHS T32HL007936NIGMS NIH HHS R01GM07054NIGMS NIH HHS R01 GM105665NIGMS NIH HHS R01 GM107054NIGMS NIH HHS T32GM008688
6 · The paper itself

Abstract

Microribonucleic acids (miRNAs) work with exquisite specificity and are able to distinguish a target from a non-target based on a single nucleotide mismatch in the core nucleotide domain. We questioned whether miRNA regulation of gene expression could occur in a single nucleotide polymorphism (SNP)-specific manner, manifesting as a post-transcriptional control of expression of genetic polymorphisms. In our recent study of the functional consequences of matrix metalloproteinase (MMP)-9 SNPs, we discovered that expression of a coding exon SNP in the pro-domain of the protein resulted in a profound decrease in the secreted protein. This missense SNP results in the N38S amino acid change and a loss of an N-glycosylation site. A systematic study demonstrated that the loss of secreted protein was due not to the loss of an N-glycosylation site, but rather an SNP-specific targeting by miR-671-3p and miR-657. Bioinformatics analysis identified 41 SNP-specific miRNA targeting MMP-9 SNPs, mostly in the coding exon and an extension of the analysis to chromosome 20, where the MMP-9 gene is located, suggesting that SNP-specific miRNAs targeting the coding exon are prevalent. This selective post-transcriptional regulation of a target messenger RNA harboring genetic polymorphisms by miRNAs offers an SNP-dependent post-transcriptional regulatory mechanism, allowing for polymorphic-specific differential gene regulation.

Indexed as

Polymorphism, Single NucleotideRNA Interference3' Untranslated RegionsAllelesBase SequenceBinding SitesEnzyme RepressionExonsGlycosylationHEK293 CellsHumansMatrix Metalloproteinase 9MicroRNAsMolecular Sequence DataMutation, MissenseOpen Reading Frames3' Untranslated RegionsMatrix Metalloproteinase 9MicroRNAsMMP9 protein, human

Identifiers

PMID24627221
PMCPMC4027190
OpenAlexW2131963674

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.